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. Author manuscript; available in PMC: 2012 Jul 11.
Published in final edited form as: Arch Intern Med. 2011 Apr 25;171(13):1150–1159. doi: 10.1001/archinternmed.2011.168

Advanced access scheduling outcomes: A systematic review

Katherine Rose 1, Joseph S Ross 2,3, Leora I Horwitz 2,3
PMCID: PMC3154021  NIHMSID: NIHMS308204  PMID: 21518935

Abstract

Background

Advanced (“open”) access scheduling, which promotes patient-driven scheduling in lieu of pre-arranged appointments, has been proposed as a more patient-centered appointment method and has been widely adopted within the United Kingdom and Veterans Health Administration and among U.S. private practices.

Objective

To describe patient, physician and practice outcomes resulting from implementation of advanced access scheduling in the primary care setting.

Data Sources

Comprehensive search of electronic databases (MEDLINE, Scopus, Web of Science) until August 2010, supplemented by reviewing reference lists and gray literature.

Study Selection

Studies were assessed blinded and in duplicate. Controlled and uncontrolled English-language studies of advanced access implementation in primary care were eligible if they specified methods and reported outcomes data.

Data Extraction

2 reviewers collaboratively assessed risk for bias by using the Cochrane Effective Practice and Organisation of Care Group Risk of Bias criteria. Data were independently extracted in duplicate.

Data Synthesis

28 papers describing 24 studies met eligibility criteria. All studies had at least one source of potential bias. All 8 studies evaluating time to third next available appointment showed reductions (range of decrease 1.1–32 days) but only 25% (2/8) achieved a third-next-available appointment <48 hours. No-show rates improved only in practices with baseline no-show rates >15%. Effects on patient satisfaction were variable. Limited data addressed clinical outcomes and loss to follow-up.

Conclusion

Studies of advanced access support benefits to wait time and no-show rate. However, effects on patient satisfaction were mixed and data about clinical outcomes and loss to follow-up were lacking.

Introduction

Advanced access is an appointment scheduling system that allows patients “to seek and receive care from the provider of choice at the time the patient chooses.”1 Traditional scheduling systems arrange appointments for future dates, resulting in each physician’s patient care time being mostly scheduled well in advance. Consequently, wait time for appointments can be long, and patients may miss long-scheduled appointments.2 In fact, the average wait time in 2009 for a new non-urgent visit with a U.S. family practice physician was 20 days.3 By contrast, in advanced access, patients are offered an appointment on the day that they call or at the time of their choosing, preferably within 24 hours. This results in few pre-scheduled appointments and a relatively open schedule. Triage is minimized as everyone is offered an appointment whether for urgent or routine care.

There has been increased interest in advanced access as waiting times for routine healthcare have lengthened in recent years,3,4 leading to negative health outcomes5 and contributing to emergency department crowding.6,7 The Institute for Healthcare Improvement reports working with about 3,000 practices to implement advanced access.8 Both the Veteran’s Affairs system and the United Kingdom’s National Health Service have implemented advanced access in their extensive networks of ambulatory practices.9,10 In 2003, 47% of National Association of Public Hospitals members reported at least piloting advanced access in their primary care clinics.11

Proponents of advanced access suggest that it reduces patient waiting times, improves continuity of care, and reduces no-shows.1214 On the other hand, skeptics of the system point out that advanced access is difficult to implement, may instead reduce continuity of care, and may leave patients with chronic conditions lost to follow-up. 11,12,15,16 Published reports of advanced access implementations are inconsistent. Therefore, given the widespread usage and promotion of advanced access, coupled with uncertainty as to its impact on physicians and patients, our objective was to summarize and evaluate the field of research examining the outcomes of advanced access scheduling systems in the primary care setting through a systematic review of the literature.

Methods

Data Sources and Searches

To identify relevant articles, we searched the following databases: OVID (1950-August 2010), Scopus (1960-August 2010), and Web of Science (1900-August 2010). Search strategies differed, depending upon the database. In OVID, we used the keywords “open access or advanc$ access or same-day” combined with the keywords “schedul$ or appoint$.” We also used the keywords “open access or advanc$ access or same-day” combined with the Medical Subject Heading (MeSH) terms “Primary Health Care” and “Appointments and Schedules” using the Boolean term “and.” In Scopus we altered the search terms to comply with search mechanisms and used (schedul* OR appoint*) AND (“open access” OR “advanced access” OR “advance access” OR “same day”). We used the search strategy TS=(schedul* OR appoint*) AND TS=(advanced access OR advance access OR open access) to identify articles in Web of Science. We also hand searched bibliographies of pertinent articles.

Study selection

Full-length articles, research letters, and brief reports in English were eligible for inclusion. Of these, we included articles that: (1) investigated an advanced access intervention in a primary care setting (including cohort, case-control, cross-sectional, and randomized controlled trials), (2) reported quantitative outcomes for patients and/or providers, and (3) compared intervention and non-intervention data. We excluded conference abstracts because of the preliminary nature of their data. Commentaries, editorials, and narratives not written in scientific format – i.e. without a full description of methodology, study population, baseline data or results, and with no statistical testing – were also excluded.

One investigator selected articles for review based on title and/or abstract. Two investigators then independently assessed abstracts for inclusion. Reviewers were blinded to author, journal, and date of publication. If an investigator could not make an inclusion/exclusion decision based on the abstract, the full article was retrieved. Disagreements were resolved by consensus.

Data Extraction and Quality Assessment

Two investigators independently extracted data for each study using a standardized form. Main outcomes included success of advanced access implementation (time to the third available appointment), physician/practice outcomes (no-show rate, fiscal outcomes, and provider satisfaction), and patient outcomes (patient satisfaction, continuity of care, loss to follow-up, emergency room/urgent care use, and chronic disease quality measures). Time-to-third-available appointment is a widely-utilized metric for appointment availability.17 It is preferred over the time to the next available appointment because it does not give the false impression of schedule availability if there is a last-minute cancellation. When time-to-third-available appointment data were reported for both new and return visits (or, long and short visits), we recorded the result for the return, or short, visit. We defined continuity of care as any measure of the frequency with which patients see their own primary care physician (PCP).1821

Studies used a variety of questions and reporting methods to describe patient satisfaction. For purposes of analysis, we divided satisfaction questions into two broad categories: overall satisfaction and appointment system satisfaction. Overall satisfaction included questions such as “How satisfied are you with today’s visit?” while appointment system satisfaction included questions such as “Were you able to get an appointment as soon as you wanted?” or “How satisfied were you with the appointment system?”

In addition, we abstracted study characteristics and demographics including trial design, funding, country of study, practice setting, number of practices and physicians, number of patients, and length of follow-up.

There are no validated tools for assessing the quality of quality improvement studies, which differ from standard therapeutic interventions in several important ways, including unit of analysis (typically provider rather than patient) and role of local context. Consequently, we adapted the Cochrane Effective Practice and Organisation of Care Group Risk of Bias criteria to qualitatively report the risk of bias of the study results.22 These criteria are similar to those found in the SQUIRE guidelines for quality improvement reporting23 and the AHRQ Evidence Report on Systems to Rate the Strength of Scientific Evidence.24 We did not consider funding as no studies were commercially funded.

Data Synthesis and Analysis

The limited reporting of the trials and wide variety of outcomes evaluated precluded a meta analysis of results; consequently, we describe results qualitatively. All study designs are reported together. We hypothesized that if advanced access were an effective strategy, then studies with more successful implementations (defined as those with shorter final time-to-third-available appointment) would be more likely to report successful physician or patient outcomes. The only outcome for which there were enough studies to examine this hypothesis was no-show rate. Consequently, to determine if the success of advance access implementation affected outcomes, we conducted a linear regression of time-to-third-available appointment on no-show rate.

We used an Access 2002 database (Microsoft, Redmond, WA) to conduct blinded, independent reviews of the literature, and SAS 9.2 (SAS Institute, Cary, NC) to conduct the linear regression. As this study did not consist of direct human subjects research, institutional review board approval was not required.

Results

The initial electronic database search identified 2,691 citations, of which 2,556 were excluded based on title review by one investigator (K.R.) because they were not about advanced access, were set in specialty settings, were conference abstracts or were duplicates found in multiple databases (Figure 1). Two independent, blinded investigators reviewed the remaining 136 article titles and abstracts for selection, excluding 74 because they were identified as not in English (N=1), not about advanced access (N=27), sub-specialty studies (N=9), reviews, editorials or non-research letters (N=29), or did not include patient or provider outcomes related to advanced access (N=8). Of the remaining 62 articles of advanced access implementations in the primary care setting that reported outcomes, 34 more were excluded because they were narratives not written in scientific format (N=31), or were qualitative studies (N=3). The resulting 28 articles are included in this systematic review. Since several interventions resulted in more than one published article, these 28 articles represented 24 distinct studies.

Figure 1.

Figure 1

Flow diagram of search results.

Characteristics of the studies are shown in Table 1. Only 1 was a randomized trial, most took place in the United States in adult medicine practices, and setting ranged from small private offices to large health systems. Follow-up ranged from three months to approximately four years.

Table 1.

Overview of included studies.

Source Provider specialty Trial design Country of study Sponsorship Provider setting Number of practices Number of providers Follow up time period
Belardi et al., 200426 Family practice Controlled before-after USA National government Teaching practice 1 (2 teams) 6 (1.3 FTE) per team 15 months
Bennett et al., 200927 * Family practice Uncontrolled before-after USA Not disclosed Teaching practice 1 49 14 months
Bundy et al., 200529 ** Family practice Uncontrolled before-after USA Non-profit Varied (1 not-for-profit practice, 1 private practice, 2 practices owned by large health system) 4 30 9 months
Dixon et al., 2006***30;
Pickin et al. 2004***32
Family practice Uncontrolled before-after UK National government National Health Service practices 462 NR 8–16 months
Kennedy et al., 200365 Family practice Uncontrolled before-after USA Not disclosed Teaching practice 1 12.8 FTE (incl non-MDs) 5 months
Meyers et al., 200339 Family practice Uncontrolled before-after USA National government US military 1 9 4 months
Phan et al., 200946 Family practice Uncontrolled before-after USA Not disclosed Teaching practice 1 32 1 year
Rohrer et al., 200747 Family practice Cross-sectional USA Not disclosed Network of community practices 4 (2 AA, 2 control) NR 1 year
Salisbury et al., 200744 and 200733;
Sampson et al., 200845;
Pickin et al. 201051
Family practice Controlled before-after UK National government National Health Service practices 48 (24 AA, 24 control) mean 3.26 FTE per practice 1 year
Mehrotra et al., 200831 Family practice and general medicine Uncontrolled before-after USA Non-profit Health system with small offices 6 (5 in analysis) 2.8–8.8 FTEs/practice 1–3 years
Armstrong, 200538 General medicine Uncontrolled before-after USA National government Veterans Affairs 862 NR 4 years
Boushon et al. 200628 General medicine Uncontrolled before-after USA Non-profit Not reported 17 NR 1 year
Lasser et al, 200536 General medicine Cross-sectional USA National government Network of neighborhood health centers 16 58 n/a
Lewandowski et al., 200666;
Solberg et al., 2004,25 and 200634; Sperl-Hillen et al, 200835
General medicine Uncontrolled before-after USA Non-profit Multispecialty medical group 17 500 all specialties; 105 (99.6 FTE) primary care 1–2 years
Lukas et al., 2004 37 General medicine Cross-sectional USA National government Veterans Affairs 78 NR n/a
Radel et al., 2001 40 *** General medicine Uncontrolled before-after USA Not disclosed Health maintenance organization 2 6 1 year
Subramanian et al., 2009 48 General medicine Controlled before-after USA National government Teaching practice 12 ~100 1 year
Cherniack et al., 2007 42 Geriatrics Uncontrolled before-after USA Not disclosed Veterans Affairs 1 8 1 year
Mallard et al., 2004 41 Pediatrics Uncontrolled before-after USA Local government Community health center 1 2 6 months
O’Connor et al., 2006 43 Pediatrics Randomized controlled trial USA National government Community health center 1 10 4 months
Parente et al., 2005 67 Pediatrics Uncontrolled before-after USA Not disclosed Teaching practice 1 4 3 months

NR, not reported; FTE, Full-time equivalent

*

Institute for Healthcare Improvement Access and Efficiency Collaborative study

**

“Institute for Healthcare Improvement QI initiative” May 2001–May 2002

***

Idealized Design of Clinical Office Practices study

The overall risk of bias in the studies was high (Appendix Tables 1 and 2). Only one study randomized physician participants, and this study was subject to substantial contamination and crossover bias. The remaining studies all included self-selected intervention groups in which baseline characteristics often differed between intervention and control groups. Furthermore at least 6 studies implemented other practice initiatives concurrently with advanced access. Less than half of studies reported basic measures of advanced access implementation such as time-to-third-available appointment.

An overview of results for each outcome is presented in Table 2. Details for each outcome follow.

Table 2.

Selected major outcomes following advanced access implementation, summary of studies

Outcome Number of studies Overall result Result among studies with concurrent control group
Time to third available appointment 8 Statistically significant improvement in 5; any improvement in all 8; only 2 achieved access < 48 hours N=2; significant improvement in both, one achieved < 48 hour access
No show rate 11 Statistically significant improvement in 5; >2% absolute improvement in 6; any improvement in 10 N=4; significant improvement in 2, non-significant change in 2
Patient satisfaction (overall) 4 Statistically significant improvement in 1; any improvement in 2 N=0
Patient satisfaction (appointments) 4 Statistically significant improvement in 0; any improvement in 2
Statistically significant worsening in 1
N=2; non-significant change in both
Continuity of care 9 Statistically significant improvement in 3; any improvement in 7
Worsening in 2 (none statistically significant)
N=3; 1 significant improvement, 2 non-significant change
Healthcare utilization 2 No significant change in ED visits or hospitalizations; 1 study reduced visits to urgent care N=1; no significant change

Wait time for an appointment

Eleven articles describing 8 studies reported time-to-third-available appointment, the preferred metric for appointment availability (Table 3).2535 Advanced access implementation was associated with a decrease in time-to-third-available appointment in all studies (range 1–32 days), and the decrease was statistically significant in all 5 studies (6 papers) in which statistical analysis was performed.2527,3234 A total of 5/8 (63%) studies achieved a mean time-to-third-available appointment of less than five days; 2 (25%) reached less than two days.32,33 One additional study of community health centers with open-access scheduling found that 49% of visits were to providers whose individual average time-to-third-available appointment was four days or less in the previous year.36 Two multisite studies found that a greater degree of advanced access implementation was significantly associated with reductions in wait time, although the effect was small.32,37 For example, in the VA, the degree of advanced access implementation accounted for 7% of the variance in wait time.37

Table 3.

Time to third available appointment

Source TTTA (days)
No-AA AA Δ in TTTA (95% CI) P-value
Belardi et al., 2004 26 21 4–7 −14 to −17 <.01
Pickin et al. 2004*32 3.6 1.9 −1.7 (−1.4 to −2.0) <.05
Bundy et al., 2005 29 36 4 −32 (−20 to −44) NR
Salisbury et al., 2007 33 2.9 1.6 −1.1 (−2.2 to −0.1) .04
Bennet and Baxley, 2009 27 30.7 9.0 −21.7 <.0001
Solberg et al., 200425 Overall 17.8 4.2 −13.6 NR
Solberg et al., 200634 Dep 19.5 4.5 −15 <.01
Sperl-Hillen et al., 200835 DM 21.6 4.2 −14.7 <.001
Mehrotra et al., 2008 31 21 11 −10 NR
Boushon et al. 2006 28 23 10 −13 NR
*

Similar results reported inDixon et al, 200630 from the same dataset

These articles report data from the same study.

TTTA, time-to-third-available appointment; AA, advanced access; Dep, depression; DM, diabetes.

Four additional studies examined time to next appointment only;3841 two of these achieved an average next-available appointment time of two days or less.39,40 The VA system as a whole, using data from over 6 million patient visits, reported an improvement in next appointment availability from 42.9 days to 15.7 days.38

Physician and practice outcomes

Besides wait time, the only practice outcome frequently studied was no-show rate, which was reported in 11 studies (Table 4). The change in no-show rate ranged from −24% to 0 and was significantly decreased in five studies.29,36,4143, Of note, three of these five studies served a population of patients with low socioeconomic status and all five had relatively high baseline no-show rates (16–43%).29,36,41

Table 4.

Physician and practice outcomes

Source No-show rate, practices without AA No-show rate, practices with AA Absolute change in no-show rate P value Visit volume, physician productivity, and compensation outcomes
Mallard et al., 200441 43% 19% −24% <.0001
  • Productivity 89%→122%, p<.0001.

  • New patient volume/month 78→95

O’Connor et al., 200643 21% 9% −12% <.02
Cherniak et al., 200742 18% 11% −9% 0
Bundy et al., 200529 16% 11% −5% (95% CI, −10 to −1) <.05
Lasser et al, 200536 17.2% 15.4% −1.8%
OR 0.80 (95% CI, 0.74 to 0.86)
<.0001
Belardi et al., 200426 8.6%→7.8% 9.2%→6.7% −2.6% NS
  • Increased RVU/pt/session 1st quarter only (1.32→1.51); then back to baseline

  • No change patients/session

  • No change panel size for AA; significant increase for traditional

Salisbury et al., 200733 4.8→4.7% 4.3→3.4% −0.9% 0.85
  • No change in patients/session (difference 1.2, 95% CI −7.1 to 9.4)

Bennett et al., 200927 19.7% 19.3% −0.4% NS
Kennedy et al., 200365 10% 6% −4% NR
  • Charges/FTE increased $11,560 to 16,844

  • Revenue/FTE increased $4,978 to $10,316

  • Visit volume “increased”

Meyers et al., 200339 Family practice: ~3.7%
Pediatrics: ~3.5%
Military medicine: ~2.9%
Internal medicine: ~1.9%
Family practice: ~2.4%
Pediatrics: ~2.9%
Military medicine: ~4%
Internal medicine: 0%
Family practice: ~−1.3%

Pediatrics: ~−0.6%
Military medicine: ~1.1%

Internal medicine: ~−1.9%
NR
Mehrotra et al., 200831 14% 14% 0% NR
Radel et al., 200140 “Financial performance improved”
Solberg et al, 2004 and 200625,34, Lewandowski et al., 200666 Office visits/patient*
 CHD 8.2→8.9, p<.0001
 DM 7.0→7.0, p=0.22
 Dep 11.4→10.9, p<.001

Total healthcare costs per person
CHD $16,631→$18736
DM $7607→$8407
Dep $6409→$7731

Financial performance
  • WRVU per FTE increased from 2,930 2 years prior to intervention to 3,980 2 years after intervention*

  • Physician production efficiency ($ paid per WRVU) decreased from $44.70 to $38.85

  • Average compensation increased from $123,581 per FTE to $148,200 per FTE

    * simultaneous change of physician payment from salary to WRVU-based system

Subramanian et al., 200948 Office visits/patient
OR 1.00 (95% CI, 0.92 to 1.08)
*

Data from Solberg 2004. In Solberg 2006, results reported as 10.8→10.4, p < 0.01.

AA, advanced access; NS, not significant; NR, not reported; FTE, full-time equivalent; RVU, relative value unit; WRVU, work relative value unit.

Seven studies reported the impact of advanced access on visit volume, physician compensation or productivity outcomes; all reported neutral to positive results (Table 4).

Patient satisfaction

Four studies reported quantitative data pertaining to overall patient satisfaction (Table 5). Of these, one reported statistically significant improvement.29 Quantitative pre/post data on satisfaction with the appointment system were presented in four studies (Table 5).29,31,37,44,45 None showed significant improvement; in one, each 10% increase in proportion of same-day appointments was associated with an 8% reduction in satisfaction (OR 0.92, 95% CI, 0.90 to 0.94).45 However, a VA survey found that patient satisfaction appeared to be higher at facilities with shorter wait times (p=0.09).37

Table 5.

Patient satisfaction and advanced access implementation

Study Satisfaction, practices without AA* Satisfaction, practices with AA* Absolute Δ satisfaction P value
Patient satisfaction: overall
Bundy et al., 2005 29 45% 61% 16% (95% CI, 0.2 to 30) <.05
Lewandowski et al., 2006 66 84% 87% 3% NS
Solberg et al., 200425 DM 36% DM 55% 19% NR
Parente et al., 2005 67 6.21 6.08 −.13 points NS
Radel et al. 200140 72%5 95% 23% NR
Patient satisfaction: appointment system
Salisbury et al. 200744, Sampson et al. 200845 52% 52% Adjusted OR 0.93 (95% CI, 0.67–1.28) NS
Bundy et al., 200529 37% 47% 10% (95% CI, −9 to 29) NS
Lukas et al., 2004 37 74% 84% 10% 0.09
Mehrotra et al., 2008 31 53% 51% −2% NR

AA, advanced access; DM, patients with diabetes only; NS, not significant; NR, not reported.

*

percent of respondents reported as “satisfied” or “highly satisfied” unless otherwise specified

Mean score on 1–7 scale with 7 = highest satisfaction

Continuity of care and loss to follow-up

The effect of advanced access scheduling on continuity of care was explored in 9 studies using multiple methods of assessing continuity (Table 6). Only two studies found significant decreases in continuity;43,46 of these, one noted that a provider in the open access group was on maternity leave during the brief 4 month period of study follow-up, potentially accounting for this finding.43

Table 6.

Clinical outcomes of advanced access

Source Continuity of care, practices without AA Continuity of care, practices with AA Change in continuity P value Urgent Care/ED/hospital use without AA→with AA Other clinical outcome
Belardi et al., 2004 26 ~75% >90% ~15% <.015
Parente et al., 2005 67 69.8% 91.4% 24.1% <.000
Solberg et al., 200425, Solberg et al, 200634, Sperl-Hillen et al., 2008 35 COC index19
CHD: 0.66
DM: 0.68
Dep: 0.60
COC index19
CHD: 0.72
DM: 0.73
Dep: 0.63

CHD: 0.06
DM: 0.05
Dep: 0.03

<.0001
<.0001
<.0001
1 or more visits to urgent care
CHD 13.5%→8.6% p<.0001
DM 17.5%→12.4% p<.0001
Dep 31.8%→22.8% p<.0001
1 or more visits to ED*
CHD 51.5%→50.9% p=0.068
DM 14.4%→15.1% p=0.078
Dep 14.9%→16.9% p=0.15
1 or more ED or urgent care visit
DM 41%→37.6%, p<.001
1 or more hospitalizations*
CHD 58.4%→57.3% p=0.002
DM 9.5%→9.7% p=0.70
Dep 7.7%→8.9% p=0.13

Mental health ED visit or hospitalization
Dep 6.5%→6.3% p=.34
Diabetes quality:
A1c <7% 44.4→52.7%
p<.001
LDL<100
29.8→38.7% p<.001

Depression quality
Continuation of new medication for 180 days
46.2%→50.8% p<.001
Phan et al., 2009 46 UPC21 0.56
MMCI20 0.49
UPC21 0.54
MMCI20 0.43
UPC21 -0.02
MMCI20 −0.06
0.13
0.001
Bundy et al., 2005 29 76% 89% 13% (95% CI, −7 to 32) NS
O’Connor et al., 2006 43 75% 60% −15% NS On-time immunization rate
74% in AA group
74% in non-AA group
Salisbury et al., 2007 33;
Pickin et al., 201051
COC index18
0.43→0.46
COC index18
0.43→0.40
Adjusted diff
.003 (−0.07 to 0.07)
0.93 Antibiotic prescribing
Reduction in monthly prescriptions of 0.9 items/1,000 patients AA relative to controls (95% CI, −2.2 to 0.4, p=0.16)
Meyers et al., 2003 39 ~38% ~45% ~7% NR
Bennett et al., 2009 27 64.0% 68.2% 4.2% NR
Subramanian et al., 200948 ED or urgent care visits
OR 0.97 (95% CI 0.92 to 1.02)
Hospitalizations
OR 0.95 (95% CI 0.81 to 1.11)
Diabetic quality
A1c −0.12% (95% CI −0.21 to −0.03)
SBP 6.4 (95% CI 5.4 to 7.5)
LDL −0.2 (95% CI −2.0 to 1.5)
Radel et al, 200140 Cardiovascular quality
LDL<100 52%→75%
HTN BP control <140/86
64%→96%

Diabetes quality
Hgb A1c ≤ 7.5
65.5%→76.6%
*

Data are from Solberg 2004. Solberg 2006 using same dataset reports 1 or more visits to the ED for depression as 25.6→27.3, p=.13 and 1 or more hospitalizations as 19.9→21.7 p<.05.

AA, advanced access; COC, continuity of care; UPC, Usual Provider Continuity Index; MMCI, Modified, Modified Continuity Index; CHD, coronary heart disease; DM, diabetes; Dep, depression; ED, emergency department; OR, odds ratio; NR, not reported; NS, reported as not significant.

Loss to follow-up was rarely evaluated and results were mixed. Two studies found no consistent difference in loss to follow-up between advanced access and traditional scheduling.26,47 One study of patients with depression found more patients had primary care follow-up after advanced access implementation (33.0% vs. 15.4%, p=.001), but also noted that fewer followed up after a mental health hospitalization (50.3% vs. 65.9%, p=.001).34 An advanced access VA practice found that 19% of geriatric patients failed to arrange follow-up appointments; however, this study did not report loss to follow-up prior to advanced access implementation.42

Clinical outcomes

Emergency Department (ED), urgent care, and/or hospitalization rates under advanced access were quantitatively reviewed in four articles about two studies (Table 6).25,34,35,48 Urgent care visits decreased significantly in one study,25 but neither study found a consistent effect on ED visits or hospitalizations.

Three studies examined clinical outcomes for diabetic patients. All found improvements in glycosylated hemoglobin control (2 statistically significant but only 1 clinically significant),35,40,48 one found significant improvement in lipid control35 and another found significant worsening of blood pressure control.48 A pre-post report of advanced access implementation in the VA reported dramatic improvement in a wide variety of clinical performance measures;38 however, the VA implemented numerous other quality improvement activities during this period which were not accounted for.49,50 A variety of other outcomes were assessed in 1–2 studies each (Table 6).

Effect of success of AA implementation on outcomes

We assessed whether outcomes were better for studies with more successful implementations (shorter time-to-third-available appointment). There was a positive but non-significant correlation between time-to-third-appointment and no show rate in the five studies reporting both measures (R2=0.69, p=0.10). We were unable to perform similar analyses for other outcomes due to lack of data.

Discussion

This systematic review investigated the impact of advanced access scheduling on no-show rates, practice finances, patient satisfaction, continuity of care, healthcare utilization and preventive care. In summary, among 28 articles describing 24 implementations, we found that the time to the third available appointment consistently decreased with advanced access scheduling, although very few studies were able to achieve same-day access. Overall, advanced access yielded neutral to small positive improvements in no-show rates, continuity and patient satisfaction, while effects on clinical outcomes were mixed. It is worth noting that these studies report outcomes of advanced access as it has been applied in the “real world.” The limited benefits we found may therefore not be attributable to a failure of the advanced access concept itself so much as imperfect implementation (as evidenced by the limited number of studies that were able to achieve same day access). Nonetheless, since most clinicians would not be likely to apply this intervention in a randomized controlled trial setting, it is useful to examine its real-world effectiveness.

Any systematic review is dependent on the quality of the studies it evaluates. The studies included in this analysis were rarely conducted in a rigorous fashion. Only one was a randomized trial and only six others had a concurrent control group. The remaining studies were conducted in a pre/post fashion without accounting for secular trends or other concurrent quality improvement initiatives, making it impossible to isolate the effect of advanced access scheduling on outcomes. This was particularly problematic for the three studies set in the Veterans Affairs system and the four studies of practices participating in Institute for Healthcare Improvement programs, in which numerous concurrent quality improvement activities were undertaken. Moreover, the limited reporting of most studies made it difficult to assess the level of advanced access achieved, while lack of statistical analysis often made it difficult to interpret the results. Very few studies included outcomes of clinical relevance.34,35,43,48,51 The wide variety of practice settings combined with the paucity of data about most outcomes prohibited us from distinguishing which effects were attributable to advanced access itself versus to local context and variability in implementation. Finally, publication bias is always of concern although we did identify both positive and negative reports.

Despite the fact that the time-to-third-available appointment declined in all studies, one of the most striking findings was the low number of practices that achieved true same-day access. Only a quarter of studies reporting time-to-third-available appointment achieved two-day access. It is possible that some of the 16 studies that did not report time-to-third-available appointment achieved successful implementations, and it is also possible that individual sites within multi-site studies may also have been successful. Nonetheless, on balance our results suggest that successful implementation of this scheduling system is challenging. Reasons provided by authors for failure included increased demand of new patients due to physician shortages, difficulty scheduling physicians to match demand, provider resistance to same-day scheduling, unexpected decreases in appointment supply due to provider illness or departure, expected changes in supply such as maternity leave and vacations, and irregular schedules of medical trainees.16,26,31 Murray and Tantau’s descriptions of advanced access do specifically describe strategies to meet these predictable roadblocks,12,13,52 yet they do not seem to have been readily overcome in practice.

No-show rates declined as time-to-third-available appointment declined. However, improvements in no-show rates were less robust than those observed in time-to-third-available appointment, and were chiefly seen in studies of underserved populations with a high baseline no-show rate. For practices with lower baseline no-show rates, advanced access did not appear to provide significant benefit. It is possible that there is a “floor” no-show rate below which improvements are unlikely. Regardless, advanced access did not provide the large benefits to no-show rates that have been theoretically postulated.

Surveys of providers show they fear that advanced access will decrease continuity if patients are encouraged to be seen immediately by whichever physician is available.16 Our results do not support this concern. Continuity of care decreased markedly in only one of 7 studies, a residency site in which irregular house staff schedules made continuity of care extremely challenging without the ability to pre-book appointments.43 Conversely, proponents of advanced access contend that the system will improve continuity by improving each provider’s availability.12,53 Our findings only partially support this theory: advanced access improved continuity in only half of the studies, and in one study, the improvement in continuity was only weakly associated with improvements in wait time.35

Despite the near-universal reduction in wait time, patient satisfaction with overall care or with the scheduling system did not consistently improve. Clinicians often assume that shorter wait times for appointments will automatically lead to improved patient satisfaction. In the VA system, patient satisfaction was positively correlated with shorter wait times.37 However, numerous surveys of patients in the UK have found that scheduling an appointment at a convenient time is more important to patients than speed of access, unless they are presenting with a new health problem.44,5456 These results are consistent among working patients, patients with chronic illness, women and older patients.55 Furthermore, one survey found that patients were no more likely to get the type of appointment they wanted (e.g. with a particular provider, provider type, or time) in the advanced access system than in practices with conventional scheduling systems.44 In fact, satisfaction decreased 8% for every 10% increase in same-day appointments available.45 Thus, a strict focus on reducing wait time for appointments by embargoing appointments – such as has been reported in the National Health Service57 – may not be a patient-centered approach to improving scheduling systems. Although this is not the intent of advanced access, which should be able to accommodate requests for appointments, qualitative studies have found that real-world implementations of advanced access often focus on same day access to the exclusion of other core principles.58

While advanced access was not designed to improve clinical outcomes per se, as with any intervention it is necessary to ensure that it does not harm patients. Additionally, since prompt care and continuity improve clinical outcomes,5962 advanced access might be expected to have clinical benefits. Few studies evaluated clinical outcomes, and here the results were mixed. Of the four studies analyzing emergency room/urgent care use, only one showed a decrease in use of these services. Diabetic care was unaffected or mildly improved.35 On-time immunization rates for children were unchanged.43 Overall then, it does not appear that advanced access in itself is a particularly robust method of improving clinical outcomes. However, we found no compelling evidence of harm.

On the other hand, we did find some evidence to support the concern that some patients may be more likely to be lost to follow-up in an advanced access system.32 In one study, nearly one fifth of geriatric patients failed to make follow-up appointments as requested, although pre-intervention data were not presented.42 While our systematic review focused on primary care only, a specialty care practice implementing advanced access noted that 50% of patients failed to call for follow-up appointments, indicating that losing patients to follow-up is of concern in specialty settings as well.63

As advanced access scheduling gains popularity, it is important to have a realistic expectation of its potential benefits.64 We found that most practices attempting advanced access reduce wait time substantially, although few achieve same-day access. For practices with high no-show rates, advanced access appears to yield marked improvements; however, it is less effective for practices with lower baseline no-show rates. Patient satisfaction does not consistently improve and may be contingent upon how the advanced access model is applied. Most importantly, data about clinical outcomes and potential harm such as loss to follow-up is lacking. A large randomized trial of open-access scheduling that includes patient outcomes such as satisfaction, continuity of care, quality of care and healthcare utilization, along with a rigorous assessment of loss to follow-up, would be valuable to further our understanding of the utility of this scheduling system.

Supplementary Material

Appendix

Acknowledgments

Funding: During the period this study was conducted, Dr. Horwitz was supported by CTSA Grant Number UL1 RR024139 from the National Center for Research Resources (NCRR), a component of the National Institutes of Health (NIH), and NIH roadmap for Medical Research. Both Dr. Ross and Dr. Horwitz are currently supported by the National Institute on Aging (K08 AG032886, K08 AG038336) and by the American Federation of Aging Research through the Paul B. Beeson Career Development Award Program. No funding source had any role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the article for publication.

This publication was made possible by CTSA Grant Number UL1 RR024139 from the National Center for Research Resources (NCRR), a component of the National Institutes of Health (NIH), and NIH roadmap for Medical Research. This project was also supported by Award Numbers K08 AG038336 and K08 AG032886 from the National Institute on Aging (NIA) and by the American Federation on Aging Research (AFAR) through the Paul B. Beeson Career Development Award Program. The contents of this publication are solely the responsibility of the authors and do not necessarily represent the official view of NCRR, NIA, AFAR or NIH. No funding source had any role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; and preparation, review, or approval of the manuscript. All authors had full access to all the data in the study. LIH takes full responsibility for the integrity of the data and the accuracy of the data analysis.

Footnotes

An earlier version of this work was presented at the Society of General Internal Medicine 31st Annual Meeting in Pittsburgh, PA, April 10, 2008.

Conflict of interest

All authors have completed the Unified Competing Interest form at www.icmje.org/coi_disclosure.pdf (available on request from the corresponding author) and declare that (1) JSR and LIH have support from the National Institute on Aging and the National Center for Research Resources for the submitted work, (2) KDR, JSR, LIH have no relationships with any company that might have an interest in the submitted work in the previous 3 years; (3) their spouses, partners, or children have no financial relationships that may be relevant to the submitted work; and (4) KDR, JSR and LIH have no non-financial interests that may be relevant to the submitted work.

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